Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs137852604
rs137852604
2 0.925 0.080 10 110228276 missense variant C/T snv 4.0E-06 7.0E-06 0.710 1.000 1 1999 1999
dbSNP: rs759049323
rs759049323
2 0.925 0.080 10 110284872 missense variant T/C;G snv 4.0E-06; 4.0E-06 0.010 1.000 1 1999 1999